Evidence map›Paper›PMID 28010897›Full record

SynthesisCritical reviews in oncology/hematology2017

Brentuximab vedotin for treatment of non-Hodgkin lymphomas: A systematic review.

Garrett K Berger, Ali McBride, Stephanie Lawson, Kelsey Royball, Seongseok Yun, Kevin Gee, Irbaz Bin Riaz, Ahlam A Saleh, Soham Puvvada, Faiz Anwer

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Critical reviews in oncology/hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.9field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 68 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Garrett K BergerCollege of Pharmacy, University of Arizona, Tucson, AZ, 85721, United States.
Ali McBrideCollege of Pharmacy, University of Arizona, Tucson, AZ, 85721, United States.
Stephanie LawsonCollege of Pharmacy, University of Arizona, Tucson, AZ, 85721, United States.
Kelsey RoyballCollege of Pharmacy, University of Arizona, Tucson, AZ, 85721, United States.
Seongseok YunDepartments of Medicine, University of Arizona, Tucson, AZ, 85721, United States.
Kevin GeeCollege of Medicine, University of Arizona, Tucson, AZ, 85721, United States.
Irbaz Bin RiazDepartments of Medicine, University of Arizona, Tucson, AZ, 85721, United States.
Ahlam A SalehUniversity of Arizona Health Sciences Library, University of Arizona, Tucson, AZ 85721, United States.
Soham PuvvadaDepartments of Medicine, University of Arizona, Tucson, AZ, 85721, United States.
Faiz AnwerHematology, Oncology, Blood & Marrow Transplantation, Department of Medicine, University of Arizona, Tucson, AZ, 85721, United States. Electronic address: anwerf@email.arizona.edu.
University of Arizona · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Teri L Bankhead · 1985 to 2026
$110.2M
Cancer Prevention and Control Translational ResearchR25CA078447 · NCI · UNIVERSITY OF ARIZONA · PI ALBERTS, DAVID SAMUEL · 1998 to 2014
$7.6M
NCI NIH HHS P30 CA023074NCI NIH HHS R25 CA078447
6 · The paper itself

Abstract

backgroundBrentuximab vedotin (BV) is an antibody-drug conjucate (ADC) comprising a CD30-directed antibody, conjugated to the microtubule-disrupting agent MMAE via a protease cleavable linker. BV is FDA approved for use in relapsed classical Hodgkin lymphoma (HL) and relapsed systemic anaplastic large cell lymphoma (sALCL). There are multiple publications for its utility in other malignancies such as diffuse large B-cell lymphoma (DLBCL), mycosis fungoides (MF), Sézary syndrome (SS), T-cell lymphomas (TCL), primary mediastinal lymphoma (PMBL), and post-transplant lymphoproliferative disorders (PTLD). We believe that BV could potentially provide a strong additional treatment option for patients suffering from NHL.

objectivePerform a systematic review on the use of BV in non-Hodgkin lymphoma (NHL) and other CD30 DATA SOURCES: We searched various databases including PubMed (1946-2015), EMBASE (1947-2015), and Cochrane Central Register of Controlled Trials (1898-2015). ELIGIBILITY CRITERIA: Inclusion criteria specified all studies and case reports of NHLs in which BV therapy was administered. INCLUDED STUDIES: A total of 28 articles met these criteria and are summarized in this manuscript.

conclusionOur findings indicate that BV induces a variety of responses, largely positive in nature and variable between NHL subtypes. With additional, properly powered prospective studies, BV may prove to be a strong candidate in the treatment of various CD30

Indexed as

Antineoplastic AgentsBrentuximab VedotinClinical Trials, Phase II as TopicHumansImmunoconjugatesLymphoma, Non-HodgkinNeoplasm Recurrence, LocalProspective StudiesAntineoplastic AgentsBrentuximab VedotinImmunoconjugatesBrentuximab vedotinCD30Relapse or refractory NHL

Identifiers

PMID28010897
PMCPMC5218629
OpenAlexW2551960109

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.